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氢自由基、氮自由基以及对流层上部臭氧的生成。

Hydrogen radicals, nitrogen radicals, and the production of O3 in the upper troposphere.

作者信息

Wennberg PO, Hanisco TF, Jaegle L, Jacob DJ, Hintsa EJ, Lanzendorf EJ, Anderson JG, Gao R, Keim ER, Donnelly SG, Negro LAD, Fahey DW, McKeen SA, Salawitch RJ, Webster CR, May RD, Herman RL, Proffitt MH, Margitan JJ, Atlas EL, Schauffler SM, Flocke F, McElroy CT, Bui TP

机构信息

P. O. Wennberg, T. F. Hanisco, E. J. Hintsa, E. J. Lanzendorf, J. G. Anderson, Department of Chemistry and Chemical Biology and Department of Earth and Planetary Sciences, Harvard University, 12 Oxford Street, Cambridge, MA 02138, USA. L. Ja.

出版信息

Science. 1998 Jan 2;279(5347):49-53. doi: 10.1126/science.279.5347.49.

Abstract

The concentrations of the hydrogen radicals OH and HO2 in the middle and upper troposphere were measured simultaneously with those of NO, O3, CO, H2O, CH4, non-methane hydrocarbons, and with the ultraviolet and visible radiation field. The data allow a direct examination of the processes that produce O3 in this region of the atmosphere. Comparison of the measured concentrations of OH and HO2 with calculations based on their production from water vapor, ozone, and methane demonstrate that these sources are insufficient to explain the observed radical concentrations in the upper troposphere. The photolysis of carbonyl and peroxide compounds transported to this region from the lower troposphere may provide the source of HOx required to sustain the measured abundances of these radical species. The mechanism by which NO affects the production of O3 is also illustrated by the measurements. In the upper tropospheric air masses sampled, the production rate for ozone (determined from the measured concentrations of HO2 and NO) is calculated to be about 1 part per billion by volume each day. This production rate is faster than previously thought and implies that anthropogenic activities that add NO to the upper troposphere, such as biomass burning and aviation, will lead to production of more O3 than expected.

摘要

对流层中层和上层中氢自由基OH和HO2的浓度与NO、O3、CO、H2O、CH4、非甲烷碳氢化合物的浓度以及紫外线和可见光辐射场同时进行了测量。这些数据使得能够直接研究在大气的这一区域中产生O3的过程。将测得的OH和HO2浓度与基于水蒸气、臭氧和甲烷产生量的计算结果进行比较表明,这些来源不足以解释对流层上层观测到的自由基浓度。从对流层下层输送到该区域的羰基和过氧化物化合物的光解可能提供维持这些自由基物种实测丰度所需的HOx来源。测量结果还说明了NO影响O3产生的机制。在所采集的对流层上层气团中,臭氧的产生速率(根据测得的HO2和NO浓度确定)经计算约为每天十亿分之一体积分数。该产生速率比之前认为的要快,这意味着向对流层上层添加NO的人为活动,如生物质燃烧和航空活动,将导致比预期更多的O3产生。

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